Impact of the Presence and Duration of Donor-Specific Antibodies on Renal Function

Abstract Background Although anti-human leukocyte antigen (HLA) antibodies (DSA) is associated with graft loss, 3 things remain unclear: whether the duration and strength of DSA affect renal function; what mean fluorescence intensity (MFI) cut-off should be used; and whether the DSA effect is additi...

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Veröffentlicht in:Transplantation proceedings 2014, Vol.46 (1), p.75-80
Hauptverfasser: Hoshino, J, Everly, M.J, Kaneku, H, Ubara, Y, Takaichi, K, Terasaki, P.I
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container_end_page 80
container_issue 1
container_start_page 75
container_title Transplantation proceedings
container_volume 46
creator Hoshino, J
Everly, M.J
Kaneku, H
Ubara, Y
Takaichi, K
Terasaki, P.I
description Abstract Background Although anti-human leukocyte antigen (HLA) antibodies (DSA) is associated with graft loss, 3 things remain unclear: whether the duration and strength of DSA affect renal function; what mean fluorescence intensity (MFI) cut-off should be used; and whether the DSA effect is additive in case of multiple DSAs. Methods A study was made of 63 patients who received living donor kidney transplants with clonal deletion protocol and were followed up for 18 months with reduced doses of immunosuppressants. DSA was tested for monthly, using Luminex Mixed and Single Antigen beads (One Lambda, Inc., Canoga Park, CA, USA). Decrease of estimated glomerular filtration rate (eGFR) was obtained at baseline and 18 months after transplantation. Association of renal damage and DSAs was compared using several DSA models with several MFI cut-offs. Results Additive DSA models always showed better association with renal damage than comprehensive models. When calculating the DSA effect in additive models, “proxy-area under the curve” (AUC)—a triangular approximation of the actual AUC—showed better association with renal damage than did DSA duration ( R 2  = 0.105 vs 0.087). Adjusting for other factors, 27% of the variation of GFR change was explained by proxy-AUC. No significant change of association occurred if the MFI cut-off level changed from 1000 to 3000. Conclusion Our results support the association of DSA with development of longitudinal renal damage. The clinical interpretation may be similar at MFI cut-offs of 1000, 2000, and 3000. An additive DSA effect may be expected in patients with multiple DSAs. Our study suggests the importance of frequently checking for DSA and reducing their MFI value to minimize renal damage by the antibodies.
doi_str_mv 10.1016/j.transproceed.2013.09.032
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Methods A study was made of 63 patients who received living donor kidney transplants with clonal deletion protocol and were followed up for 18 months with reduced doses of immunosuppressants. DSA was tested for monthly, using Luminex Mixed and Single Antigen beads (One Lambda, Inc., Canoga Park, CA, USA). Decrease of estimated glomerular filtration rate (eGFR) was obtained at baseline and 18 months after transplantation. Association of renal damage and DSAs was compared using several DSA models with several MFI cut-offs. Results Additive DSA models always showed better association with renal damage than comprehensive models. When calculating the DSA effect in additive models, “proxy-area under the curve” (AUC)—a triangular approximation of the actual AUC—showed better association with renal damage than did DSA duration ( R 2  = 0.105 vs 0.087). Adjusting for other factors, 27% of the variation of GFR change was explained by proxy-AUC. No significant change of association occurred if the MFI cut-off level changed from 1000 to 3000. Conclusion Our results support the association of DSA with development of longitudinal renal damage. The clinical interpretation may be similar at MFI cut-offs of 1000, 2000, and 3000. An additive DSA effect may be expected in patients with multiple DSAs. Our study suggests the importance of frequently checking for DSA and reducing their MFI value to minimize renal damage by the antibodies.</description><identifier>ISSN: 0041-1345</identifier><identifier>EISSN: 1873-2623</identifier><identifier>DOI: 10.1016/j.transproceed.2013.09.032</identifier><identifier>PMID: 24507029</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adult ; Antibodies - immunology ; Area Under Curve ; Female ; Fluorescence ; Glomerular Filtration Rate ; Histocompatibility Testing - methods ; HLA Antigens - immunology ; Humans ; Immunosuppressive Agents - therapeutic use ; Kidney - immunology ; Kidney Transplantation ; Living Donors ; Male ; Models, Statistical ; Renal Insufficiency - immunology ; Renal Insufficiency - surgery ; Surgery ; Time Factors ; Young Adult</subject><ispartof>Transplantation proceedings, 2014, Vol.46 (1), p.75-80</ispartof><rights>Elsevier Inc.</rights><rights>2014 Elsevier Inc.</rights><rights>Copyright © 2014 Elsevier Inc. 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Methods A study was made of 63 patients who received living donor kidney transplants with clonal deletion protocol and were followed up for 18 months with reduced doses of immunosuppressants. DSA was tested for monthly, using Luminex Mixed and Single Antigen beads (One Lambda, Inc., Canoga Park, CA, USA). Decrease of estimated glomerular filtration rate (eGFR) was obtained at baseline and 18 months after transplantation. Association of renal damage and DSAs was compared using several DSA models with several MFI cut-offs. Results Additive DSA models always showed better association with renal damage than comprehensive models. When calculating the DSA effect in additive models, “proxy-area under the curve” (AUC)—a triangular approximation of the actual AUC—showed better association with renal damage than did DSA duration ( R 2  = 0.105 vs 0.087). Adjusting for other factors, 27% of the variation of GFR change was explained by proxy-AUC. No significant change of association occurred if the MFI cut-off level changed from 1000 to 3000. Conclusion Our results support the association of DSA with development of longitudinal renal damage. The clinical interpretation may be similar at MFI cut-offs of 1000, 2000, and 3000. An additive DSA effect may be expected in patients with multiple DSAs. Our study suggests the importance of frequently checking for DSA and reducing their MFI value to minimize renal damage by the antibodies.</description><subject>Adult</subject><subject>Antibodies - immunology</subject><subject>Area Under Curve</subject><subject>Female</subject><subject>Fluorescence</subject><subject>Glomerular Filtration Rate</subject><subject>Histocompatibility Testing - methods</subject><subject>HLA Antigens - immunology</subject><subject>Humans</subject><subject>Immunosuppressive Agents - therapeutic use</subject><subject>Kidney - immunology</subject><subject>Kidney Transplantation</subject><subject>Living Donors</subject><subject>Male</subject><subject>Models, Statistical</subject><subject>Renal Insufficiency - immunology</subject><subject>Renal Insufficiency - surgery</subject><subject>Surgery</subject><subject>Time Factors</subject><subject>Young Adult</subject><issn>0041-1345</issn><issn>1873-2623</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkU9P3DAQxa2qqCyUr1BFnHpJGP_JJumhEtplYSUkEJSz5Thj1dusvbUTJL49jnaRECdOI-u9mfH7DSHnFAoKdH6xKYagXNwFrxG7ggHlBTQFcPaFzGhd8ZzNGf9KZgCC5pSL8picxLiB9GaCfyPHTJRQAWtm5GG93Sk9ZN5kw1_M7gNGdBoz5bpsOQY1WO8mcemdD_njDrU1VmeXbrCt7yzGLOkP6FSfrUanJ_t3cmRUH_HsUE_J0-rqz-Imv727Xi8ub3MteDnkylRNPUdgHTcoBNTAoK7aRlUl0vRB2mqjhRJGVFjzuhYGVNm1jJtOV3XD-Cn5uZ-bQPwfMQ5ya6PGvlcO_RglFU2Twqegyfprb9XBxxjQyF2wWxVeJAU5MZUb-Z6pnJhKaGRimpp_HPaM7TZpb61vEJNhuTdgSvtsMcio7USxswH1IDtvP7fn94cxurfOatX_wxeMGz-GhDnlkpFJkI_TdafjUg6UslReAWqTowM</recordid><startdate>2014</startdate><enddate>2014</enddate><creator>Hoshino, J</creator><creator>Everly, M.J</creator><creator>Kaneku, H</creator><creator>Ubara, Y</creator><creator>Takaichi, K</creator><creator>Terasaki, P.I</creator><general>Elsevier Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope></search><sort><creationdate>2014</creationdate><title>Impact of the Presence and Duration of Donor-Specific Antibodies on Renal Function</title><author>Hoshino, J ; Everly, M.J ; Kaneku, H ; Ubara, Y ; Takaichi, K ; Terasaki, P.I</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c435t-af7986e02d3fe440802087b9a75e12451bcfc4a4f47e83884f0a5db23fdc78923</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Adult</topic><topic>Antibodies - immunology</topic><topic>Area Under Curve</topic><topic>Female</topic><topic>Fluorescence</topic><topic>Glomerular Filtration Rate</topic><topic>Histocompatibility Testing - methods</topic><topic>HLA Antigens - immunology</topic><topic>Humans</topic><topic>Immunosuppressive Agents - therapeutic use</topic><topic>Kidney - immunology</topic><topic>Kidney Transplantation</topic><topic>Living Donors</topic><topic>Male</topic><topic>Models, Statistical</topic><topic>Renal Insufficiency - immunology</topic><topic>Renal Insufficiency - surgery</topic><topic>Surgery</topic><topic>Time Factors</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hoshino, J</creatorcontrib><creatorcontrib>Everly, M.J</creatorcontrib><creatorcontrib>Kaneku, H</creatorcontrib><creatorcontrib>Ubara, Y</creatorcontrib><creatorcontrib>Takaichi, K</creatorcontrib><creatorcontrib>Terasaki, P.I</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><jtitle>Transplantation proceedings</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hoshino, J</au><au>Everly, M.J</au><au>Kaneku, H</au><au>Ubara, Y</au><au>Takaichi, K</au><au>Terasaki, P.I</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Impact of the Presence and Duration of Donor-Specific Antibodies on Renal Function</atitle><jtitle>Transplantation proceedings</jtitle><addtitle>Transplant Proc</addtitle><date>2014</date><risdate>2014</risdate><volume>46</volume><issue>1</issue><spage>75</spage><epage>80</epage><pages>75-80</pages><issn>0041-1345</issn><eissn>1873-2623</eissn><abstract>Abstract Background Although anti-human leukocyte antigen (HLA) antibodies (DSA) is associated with graft loss, 3 things remain unclear: whether the duration and strength of DSA affect renal function; what mean fluorescence intensity (MFI) cut-off should be used; and whether the DSA effect is additive in case of multiple DSAs. Methods A study was made of 63 patients who received living donor kidney transplants with clonal deletion protocol and were followed up for 18 months with reduced doses of immunosuppressants. DSA was tested for monthly, using Luminex Mixed and Single Antigen beads (One Lambda, Inc., Canoga Park, CA, USA). Decrease of estimated glomerular filtration rate (eGFR) was obtained at baseline and 18 months after transplantation. Association of renal damage and DSAs was compared using several DSA models with several MFI cut-offs. Results Additive DSA models always showed better association with renal damage than comprehensive models. When calculating the DSA effect in additive models, “proxy-area under the curve” (AUC)—a triangular approximation of the actual AUC—showed better association with renal damage than did DSA duration ( R 2  = 0.105 vs 0.087). Adjusting for other factors, 27% of the variation of GFR change was explained by proxy-AUC. No significant change of association occurred if the MFI cut-off level changed from 1000 to 3000. Conclusion Our results support the association of DSA with development of longitudinal renal damage. The clinical interpretation may be similar at MFI cut-offs of 1000, 2000, and 3000. An additive DSA effect may be expected in patients with multiple DSAs. Our study suggests the importance of frequently checking for DSA and reducing their MFI value to minimize renal damage by the antibodies.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>24507029</pmid><doi>10.1016/j.transproceed.2013.09.032</doi><tpages>6</tpages></addata></record>
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subjects Adult
Antibodies - immunology
Area Under Curve
Female
Fluorescence
Glomerular Filtration Rate
Histocompatibility Testing - methods
HLA Antigens - immunology
Humans
Immunosuppressive Agents - therapeutic use
Kidney - immunology
Kidney Transplantation
Living Donors
Male
Models, Statistical
Renal Insufficiency - immunology
Renal Insufficiency - surgery
Surgery
Time Factors
Young Adult
title Impact of the Presence and Duration of Donor-Specific Antibodies on Renal Function
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